Taiwan FDA registration 158e03c528d0e0799ff5f3b530a8aa53
"SHIE-TUNG" Keratoscope (Non-Sterile)
TW: "協同" 角膜鏡 (未滅菌)
Taiwan·Risk Class 1·MD·US OPHTHALMIC·Registered Aug 12, 2016 – Aug 12, 2021ExpiredRegistration details
- Analysis ID
- 158e03c528d0e0799ff5f3b530a8aa53
- License Form
- Ministry of Health Medical Device Import No. 016893
- Customs Code
- DHA09401689309
Company information
- Manufacturer
- US OPHTHALMIC
- Manufacturer Country
- United States
- Authorized Representative
- Synergy Optics Ltd
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 12, 2016
- Expiry Date
- Aug 12, 2021
About this record
Access comprehensive regulatory information for "SHIE-TUNG" Keratoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 158e03c528d0e0799ff5f3b530a8aa53 and manufactured by US OPHTHALMIC. The authorized representative in Taiwan is Synergy Optics Ltd.
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